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Origin of Shrinkage

Wood-Plastic Composites, by Anatole A. Klyosov Copyright 2007 John Wiley Sons, Inc. [Pg.333]

LINEAR SHRINKAGE OF EXTRUDED WOOD-PLASTIC COMPOSITES [Pg.334]

This configuration includes as many internal interactions as possible ( secondary structure ), and as a result it is randomly coiled, or folded into a shape resembling a bean. This might be called a tertiary structure.  [Pg.334]

In a solid state and in a hot melt, being still or moving slowly, polyethylene molecules preserve this bean shape. Besides, in the solid state HDPE is a semicrystalline polymer, that is it contains both well-packed, crystalline areas and amorphous regions (Fig. 9.2). [Pg.334]

In a hot melt, of course, crystals are molten. However, the faster the hot melt flows, the more elongated (aligned) the polyethylene molecules become in the direction of [Pg.334]


Reverse segregation 3. Contrary to the solute distribution of positive segregation, the originations of shrinkage that the high concentration liquid of solute in the center is squeezed to the surface when they are transmitted through the channel of the dendrite. [Pg.330]

Fig. 6. Illustration for the origin of the shrinkage effect in MXj moiecuies is the equilibrium X X distance, r is the instantaneous X X distance during vibration. Because of the perpendic-uiar (bending) vibrations, the average internuciear distance, fg = / r i)P(y) d7 is less than the equilibrium distance here P(y)dy expresses the protebility that the angle X-M-X lies between y and y + dy... Fig. 6. Illustration for the origin of the shrinkage effect in MXj moiecuies is the equilibrium X X distance, r is the instantaneous X X distance during vibration. Because of the perpendic-uiar (bending) vibrations, the average internuciear distance, fg = / r i)P(y) d7 is less than the equilibrium distance here P(y)dy expresses the protebility that the angle X-M-X lies between y and y + dy...
The monomer can be heated in the presence of an initiator giving a clear plastic shaped like the container, but a little smaller because of shrinkage. The volume of the monomers is generally larger than the final polymers thus, the density of the polymer is greater than that of the original monomer. [Pg.186]

An alternative theory, first proposed by Rettori and Villain (1988). takes the point of view which corresponds to the variation depicted in Fig. 1 (a), in which case the excess chemical potential of the top terrace is much lower than Eq. (6) suggests. In fact, in their treatment, the shrinkage of the top terrace is drivrii by the pressure from the step trains on either side, which has its origin in the repulsive interaction (of elastic or entropic origin) of like steps. This yields an effective chemical potential for the top terrace,... [Pg.172]

There are many controversial opinions as the origin of microcracks is concerned, because this phenomenon depends on many factors related both to the properties of concrete and to the environmental. Particularly the significance is attributed to the shrinkage affecting factors therefore the number of microcracks grows with fineness, as well as with the cement soluble alkali content, and presumably, with CjA content, particularly above 8% [3],... [Pg.374]

The large thickness and relaxation character of the IL in samples used favoured the "mechanical origin of the IL during the formation of coatings. A "mechanical" IL is not important, but a sone of a polymer, excited by a substrate, i.e. it is a result of the resistance of the solid phase, whose volume is constant, to the shrinkage stress in a polymer component. On the other hand a "mechanical" IL is a sone of the localization of inner stretching stresses at the interface. [Pg.432]

The volumetric shrinkage of peat increases up to a maximum and then remains constant, the volume being reduced almost to the point of complete dehydration. The amount of shrinkage that can occur generally ranges between 10 and 75% of the original volume of the peat, and it can involve reductions in void ratio from over 12 down to about 2. [Pg.247]

Sanfor-set trademark. A trademark of Cluett, Peabody Co. Inc., denoting a controlled standard of shrinkage performance originally developed for denims. Fabrics bearing this trademark will not shrink under home-wash, tumble-dry conditions because they have been subjected to a liquid ammonia treatment and compressive shrinkage. [Pg.858]


See other pages where Origin of Shrinkage is mentioned: [Pg.333]    [Pg.335]    [Pg.338]    [Pg.385]    [Pg.333]    [Pg.335]    [Pg.338]    [Pg.385]    [Pg.257]    [Pg.1196]    [Pg.470]    [Pg.371]    [Pg.296]    [Pg.220]    [Pg.779]    [Pg.257]    [Pg.188]    [Pg.814]    [Pg.1019]    [Pg.623]    [Pg.166]    [Pg.539]    [Pg.202]    [Pg.492]    [Pg.1385]    [Pg.64]    [Pg.98]    [Pg.587]    [Pg.118]    [Pg.174]    [Pg.129]    [Pg.131]    [Pg.455]    [Pg.1384]    [Pg.521]    [Pg.1200]    [Pg.141]    [Pg.64]    [Pg.341]    [Pg.535]    [Pg.667]    [Pg.371]    [Pg.436]    [Pg.212]    [Pg.236]    [Pg.55]   


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Shrinkage

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